AIM - Nitrogen heterocycles address a favored theme in regular items and organically dynamic compounds 9, as such synthetic chemists have since quite a while ago centered their endeavors around the functionalization also, development of these significant ring frameworks. In this respect, advancements in the field of photoredox catalysis have conveyed a wide cluster of manufactured procedures for site selective a functionalization of amines. Established upon early work from the Stephenson group, who uncovered a photoredox-catalyzed aza Henry reaction in 2010 (Scheme 3), 10 an overall oxidative activation mode has emerged for N-arylamines. In these changes, reductive extinguishing of the energized condition of the photocatalyst by an amine produces an amine radical cation. Give the reaction oxidative alpha amino reaction through intramolecular cylization